Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Jessica Mandrioli

Showing results (41-50 of 177) with videos related to

Pageof 18
Sort By:
Biomolecules|September 28, 2024
Reduced Levels of Neurosteroids in Cerebrospinal Fluid of Amyotrophic Lateral Sclerosis PatientsChiara Lucchi, Cecilia Simonini, Cecilia Rustichelli, et al.
Neural Regeneration Research|May 20, 2024
Multifaceted superoxide dismutase 1 expression in amyotrophic lateral sclerosis patients: a rare occurrence?Ilaria Martinelli, Jessica Mandrioli, Andrea Ghezzi, et al.
Amyotrophic Lateral Sclerosis : Official Publication of the World Federation of Neurology Research Group on Motor Neuron Diseases|December 17, 2009
Comment on 'Huntington's disease presenting as ALS'Jessica Mandrioli, Chiara Bernabei, Eleni Georgoulopoulou, et al.
Journal of Neuroinflammation|June 2, 2016
Reduced levels of alpha-1-antitrypsin in cerebrospinal fluid of amyotrophic lateral sclerosis patients: a novel approach for a potential treatmentUri Wormser, Jessica Mandrioli, Marco Vinceti, et al.
Brain, Behavior, and Immunity|August 25, 2024
Long-term survival of participants in a phase II randomized trial of RNS60 in amyotrophic lateral sclerosisElisabetta Pupillo, Elisa Bianchi, Valentina Bonetto, et al.
Archives of Neurology|July 14, 2010
Bilateral vocal cord paralysis: a rare onset of amyotrophic lateral sclerosisGuido Bigliardi, Maria Chiara Malaguti, Patrizia Sola, et al.
Neurobiology of Aging|June 29, 2022
G507D mutation in FUS gene causes familial amyotrophic lateral sclerosis with a specific genotype-phenotype correlationIlaria Martinelli, Elisabetta Zucchi, Viviana Pensato, et al.
Amyotrophic Lateral Sclerosis : Official Publication of the World Federation of Neurology Research Group on Motor Neuron Diseases|February 2, 2012
Founder effect hypothesis of D11Y SOD1 mutation in Italian amyotrophic lateral sclerosis patientsSerena Lattante, Giuseppe Marangi, Marco Luigetti, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|April 19, 2011
Isolated progressive cognitive impairment and depression in a patient with neuroradiological features suggestive of multiple sclerosisDiana Ferraro, Anna Maria Simone, Elisa Merelli, et al.
Neurotoxicology|June 5, 2013
Cerebrospinal fluid of newly diagnosed amyotrophic lateral sclerosis patients exhibits abnormal levels of selenium species including elevated seleniteMarco Vinceti, Nikolay Solovyev, Jessica Mandrioli, et al.
Pageof 18

Showing results (41-50 of 177) with videos related to

Sort By:
Pageof 18
Biomolecules|September 28, 2024
Reduced Levels of Neurosteroids in Cerebrospinal Fluid of Amyotrophic Lateral Sclerosis PatientsChiara Lucchi, Cecilia Simonini, Cecilia Rustichelli, et al.
Neural Regeneration Research|May 20, 2024
Multifaceted superoxide dismutase 1 expression in amyotrophic lateral sclerosis patients: a rare occurrence?Ilaria Martinelli, Jessica Mandrioli, Andrea Ghezzi, et al.
Amyotrophic Lateral Sclerosis : Official Publication of the World Federation of Neurology Research Group on Motor Neuron Diseases|December 17, 2009
Comment on 'Huntington's disease presenting as ALS'Jessica Mandrioli, Chiara Bernabei, Eleni Georgoulopoulou, et al.
Journal of Neuroinflammation|June 2, 2016
Reduced levels of alpha-1-antitrypsin in cerebrospinal fluid of amyotrophic lateral sclerosis patients: a novel approach for a potential treatmentUri Wormser, Jessica Mandrioli, Marco Vinceti, et al.
Brain, Behavior, and Immunity|August 25, 2024
Long-term survival of participants in a phase II randomized trial of RNS60 in amyotrophic lateral sclerosisElisabetta Pupillo, Elisa Bianchi, Valentina Bonetto, et al.
Archives of Neurology|July 14, 2010
Bilateral vocal cord paralysis: a rare onset of amyotrophic lateral sclerosisGuido Bigliardi, Maria Chiara Malaguti, Patrizia Sola, et al.
Neurobiology of Aging|June 29, 2022
G507D mutation in FUS gene causes familial amyotrophic lateral sclerosis with a specific genotype-phenotype correlationIlaria Martinelli, Elisabetta Zucchi, Viviana Pensato, et al.
Amyotrophic Lateral Sclerosis : Official Publication of the World Federation of Neurology Research Group on Motor Neuron Diseases|February 2, 2012
Founder effect hypothesis of D11Y SOD1 mutation in Italian amyotrophic lateral sclerosis patientsSerena Lattante, Giuseppe Marangi, Marco Luigetti, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|April 19, 2011
Isolated progressive cognitive impairment and depression in a patient with neuroradiological features suggestive of multiple sclerosisDiana Ferraro, Anna Maria Simone, Elisa Merelli, et al.
Neurotoxicology|June 5, 2013
Cerebrospinal fluid of newly diagnosed amyotrophic lateral sclerosis patients exhibits abnormal levels of selenium species including elevated seleniteMarco Vinceti, Nikolay Solovyev, Jessica Mandrioli, et al.
Pageof 18